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杜氏盐藻胡萝卜素对F344大鼠的亚慢性毒性研究。

A subchronic toxicity study of dunaliella carotene in F344 rats.

作者信息

Kuroiwa Y, Nishikawa A, Imazawa T, Kitamura Y, Kanki K, Ishii Y, Umemura T, Hirose M

机构信息

Division of Pathology, National Institute of Health Sciences, Setagaya-ku, Tokyo, Japan.

出版信息

Food Chem Toxicol. 2006 Jan;44(1):138-45. doi: 10.1016/j.fct.2005.06.010. Epub 2005 Aug 10.

DOI:10.1016/j.fct.2005.06.010
PMID:16095791
Abstract

Dunaliella carotene, extracted from dunaliella alga (Dunaliella bardawil or Dunaliella salina), for use as a food-coloring agent, has beta-carotene as its mainly constituent. As there have been no reports of toxicological evaluation, a 90-day subchronic toxicity study was here performed in F344 rats at dose levels of 0 (control), 0.63%, 1.25%, 2.5% and 5% in powdered basal diet. The average daily intakes of dunaliella carotene were 352, 696, 1420 and 2750 mg/kg/day, respectively, for males, and 370, 748, 1444 and 2879 mg/kg/day for females. No mortality or treatment-related clinical signs were observed throughout the experimental period in any of the groups. Body weight gain was slightly but significantly (p < 0.05) reduced from week 5 to the end of the experiment in 2.5% and 5% males. Increased PLT were observed in 1.25% and 5% males, and 2.5% and 5% females. Significant elevations or tendencies for increase in serum T. Cho and Ca were observed in all treated males and females, with clear dose-dependence in males. Organ weight measurement and histopathological observation revealed no toxicological changes. Based on growth suppression, no-observed-adverse-effect-levels (NOAELs) were estimated to be 1.25% (696 mg/kg/day) for males and 5% (2879 mg/kg/day) for females. As increases in serum Ca were observed in the lowest group in both sexes, a no-observed-effect level (NOEL) could not be determined in this study.

摘要

从盐生杜氏藻(巴氏杜氏藻或盐生杜氏藻)中提取的杜氏藻胡萝卜素用作食用色素,其主要成分是β-胡萝卜素。由于尚无毒理学评价报告,因此在此对F344大鼠进行了为期90天的亚慢性毒性研究,在粉状基础日粮中设置了0(对照)、0.63%、1.25%、2.5%和5%的剂量水平。雄性大鼠杜氏藻胡萝卜素的平均日摄入量分别为352、696、1420和2750毫克/千克/天,雌性大鼠分别为370、748、1444和2879毫克/千克/天。在整个实验期间,任何组均未观察到死亡或与处理相关的临床体征。在2.5%和5%剂量组的雄性大鼠中,从第5周直到实验结束,体重增加略有减少但差异显著(p<0.05)。在1.25%和5%剂量组的雄性大鼠以及2.5%和5%剂量组的雌性大鼠中观察到血小板(PLT)增加。在所有接受处理的雄性和雌性大鼠中均观察到血清总胆固醇(T.Cho)和钙显著升高或有升高趋势,在雄性大鼠中具有明显的剂量依赖性。器官重量测量和组织病理学观察未发现毒理学变化。基于生长抑制情况,估计雄性大鼠的无观察到有害作用水平(NOAELs)为1.25%(696毫克/千克/天),雌性大鼠为5%(2879毫克/千克/天)。由于在最低剂量组的两性中均观察到血清钙升高,因此本研究无法确定无观察到作用水平(NOEL)。

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